IL-31 Serum Protein and Tissue rnRNA Levels in Patients with Atopic Dermatitis

被引:51
作者
Kim, Song [1 ]
Kim, Hyun-Je [1 ]
Yang, Hee Seung [2 ]
Kim, Eugene [1 ]
Huh, Ik-Soo [3 ]
Yang, Jun-Mo [1 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Dept Dermatol, Samsung Med Ctr, Seoul 135710, South Korea
[2] Brown Univ, Providence, RI 02912 USA
[3] Seoul Natl Univ, Dept Stat, Seoul, South Korea
关键词
Atopic dermatitis; IL-31; mRNA; Itching; SCORAD; Serum IL-31; T-CELLS; GENE-EXPRESSION; LESIONAL SKIN; NC/NGA MICE; PRURITUS; SEVERITY; MODEL; ITCH;
D O I
10.5021/ad.2011.23.4.468
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Severe pruritus is the primary symptom in atopic dermatitis (AD). Recently, the novel cytokine IL-31 has been implicated in the itching associated with AD. Objective: We performed this study to determine whether IL-31 serum levels are elevated in AD patients and to better characterize the relationship between serum IL-31 level and other established laboratory parameters. Methods: We recruited 55 AD patients, 34 with allergic type AD and 21 with non-allergic type AD, and 38 healthy, non-atopic controls. We checked the laboratory values, severity score, and serum IL-31 levels in all patients and controls, and IL-31 mRNA levels in lesion skin were measured in 13 subjects with AD and in four controls. Results: AD patients displayed significantly higher levels of serum IL-31 that were associated with serum IgE, disease severity, and subjective itch intensity. In AD patients, IL-31 mRNA levels from the lesional skin samples also correlated with serum IL-31 level. Conclusion: IL-31 is likely one of the many mediators inducing inflammation and pruritus in AD. Although our limited sample size prevents us from making any definitive conclusions, our data demonstrate a strong correlation between IL-31 mRNA level and serum IL-31 protein level, which has never been reported before. Moreover, we found correlations between serum IL-31 level and serum IgE, eosinophil cationic protein, disease severity, and subject itch intensity in certain degrees in AD patients. (Ann Dermatol 23(4) 468 similar to 473, 2011)
引用
收藏
页码:468 / 473
页数:6
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